TWI334867B - Therapeutic compounds - Google Patents

Therapeutic compounds Download PDF

Info

Publication number: TWI334867B
Authority: TW; Taiwan
Prior art keywords: group; cr9r10; compound; independently selected; aryl
Prior art date: 2006-07-05

Application number

TW096124262A

Other languages

English (en)

Chinese (zh)

Other versions

TW200811159A (en

Inventor

Simon Paul Planken

Scott Channing Sutton

Rongliang Chen

Original Assignee

Pfizer Prod Inc

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2006-07-05

Filing date

2007-07-04

Publication date

2010-12-21

2007-07-04 Application filed by Pfizer Prod Inc filed Critical Pfizer Prod Inc

2008-03-01 Publication of TW200811159A publication Critical patent/TW200811159A/zh

2010-12-21 Application granted granted Critical

2010-12-21 Publication of TWI334867B publication Critical patent/TWI334867B/zh

Links

150000001875 compounds Chemical class 0.000 title claims description 459
230000001225 therapeutic effect Effects 0.000 title description 4
229910052739 hydrogen Inorganic materials 0.000 claims description 367
-1 C3-C8 ring Chemical group 0.000 claims description 188
239000001257 hydrogen Substances 0.000 claims description 146
239000000203 mixture Substances 0.000 claims description 146
125000001072 heteroaryl group Chemical group 0.000 claims description 143
125000000623 heterocyclic group Chemical group 0.000 claims description 143
150000003839 salts Chemical class 0.000 claims description 114
125000000217 alkyl group Chemical group 0.000 claims description 112
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 109
125000003118 aryl group Chemical group 0.000 claims description 86
150000002431 hydrogen Chemical class 0.000 claims description 76
239000012453 solvate Substances 0.000 claims description 73
125000005843 halogen group Chemical group 0.000 claims description 62
241000124008 Mammalia Species 0.000 claims description 59
125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 claims description 57
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 54
DLFVBJFMPXGRIB-UHFFFAOYSA-N thioacetamide Natural products CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 claims description 52
125000000753 cycloalkyl group Chemical group 0.000 claims description 48
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 46
125000000041 C6-C10 aryl group Chemical group 0.000 claims description 38
OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 38
125000002534 ethynyl group Chemical group [H]C#C* 0.000 claims description 35
239000008194 pharmaceutical composition Substances 0.000 claims description 34
229910052757 nitrogen Inorganic materials 0.000 claims description 27
239000003814 drug Substances 0.000 claims description 25
239000002904 solvent Substances 0.000 claims description 23
102000002004 Cytochrome P-450 Enzyme System Human genes 0.000 claims description 21
108010015742 Cytochrome P-450 Enzyme System Proteins 0.000 claims description 21
AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 claims description 21
238000002360 preparation method Methods 0.000 claims description 21
125000004093 cyano group Chemical group *C#N 0.000 claims description 20
125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 20
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 20
239000004030 hiv protease inhibitor Substances 0.000 claims description 17
239000003112 inhibitor Substances 0.000 claims description 17
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 16
NIHNNTQXNPWCJQ-UHFFFAOYSA-N fluorene Chemical compound C1=CC=C2CC3=CC=CC=C3C2=C1 NIHNNTQXNPWCJQ-UHFFFAOYSA-N 0.000 claims description 15
150000001412 amines Chemical class 0.000 claims description 14
125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 claims description 14
MHZGKXUYDGKKIU-UHFFFAOYSA-N Decylamine Chemical compound CCCCCCCCCCN MHZGKXUYDGKKIU-UHFFFAOYSA-N 0.000 claims description 13
230000002401 inhibitory effect Effects 0.000 claims description 13
230000036436 anti-hiv Effects 0.000 claims description 12
GTCAXTIRRLKXRU-UHFFFAOYSA-N methyl carbamate Chemical compound COC(N)=O GTCAXTIRRLKXRU-UHFFFAOYSA-N 0.000 claims description 12
239000004202 carbamide Substances 0.000 claims description 11
239000003937 drug carrier Substances 0.000 claims description 11
230000004060 metabolic process Effects 0.000 claims description 11
125000004433 nitrogen atom Chemical group N* 0.000 claims description 11
239000002259 anti human immunodeficiency virus agent Substances 0.000 claims description 10
229940124411 anti-hiv antiviral agent Drugs 0.000 claims description 10
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 10
125000004076 pyridyl group Chemical group 0.000 claims description 10
239000013543 active substance Substances 0.000 claims description 9
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 9
125000001424 substituent group Chemical group 0.000 claims description 9
QUSNBJAOOMFDIB-UHFFFAOYSA-N Ethylamine Chemical compound CCN QUSNBJAOOMFDIB-UHFFFAOYSA-N 0.000 claims description 8
229910052707 ruthenium Inorganic materials 0.000 claims description 8
239000011734 sodium Substances 0.000 claims description 8
125000000339 4-pyridyl group Chemical group N1=C([H])C([H])=C([*])C([H])=C1[H] 0.000 claims description 7
KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical group C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims description 7
KJTLSVCANCCWHF-UHFFFAOYSA-N Ruthenium Chemical compound [Ru] KJTLSVCANCCWHF-UHFFFAOYSA-N 0.000 claims description 7
229910052708 sodium Inorganic materials 0.000 claims description 7
VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 7
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 claims description 6
WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 claims description 6
229910052736 halogen Inorganic materials 0.000 claims description 6
125000005842 heteroatom Chemical group 0.000 claims description 6
VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 6
239000003419 rna directed dna polymerase inhibitor Substances 0.000 claims description 6
102100035875 C-C chemokine receptor type 5 Human genes 0.000 claims description 5
101710149870 C-C chemokine receptor type 5 Proteins 0.000 claims description 5
125000004648 C2-C8 alkenyl group Chemical group 0.000 claims description 5
125000004649 C2-C8 alkynyl group Chemical group 0.000 claims description 5
108010078851 HIV Reverse Transcriptase Proteins 0.000 claims description 5
239000000460 chlorine Substances 0.000 claims description 5
125000002883 imidazolyl group Chemical group 0.000 claims description 5
125000000714 pyrimidinyl group Chemical group 0.000 claims description 5
CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical group FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 claims description 5
125000000304 alkynyl group Chemical group 0.000 claims description 4
229960005475 antiinfective agent Drugs 0.000 claims description 4
239000004599 antimicrobial Substances 0.000 claims description 4
125000002704 decyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 4
150000002367 halogens Chemical class 0.000 claims description 4
125000003226 pyrazolyl group Chemical group 0.000 claims description 4
CNPVJJQCETWNEU-CYFREDJKSA-N (4,6-dimethyl-5-pyrimidinyl)-[4-[(3S)-4-[(1R)-2-methoxy-1-[4-(trifluoromethyl)phenyl]ethyl]-3-methyl-1-piperazinyl]-4-methyl-1-piperidinyl]methanone Chemical compound N([C@@H](COC)C=1C=CC(=CC=1)C(F)(F)F)([C@H](C1)C)CCN1C(CC1)(C)CCN1C(=O)C1=C(C)N=CN=C1C CNPVJJQCETWNEU-CYFREDJKSA-N 0.000 claims description 3
125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims description 3
125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims description 3
ZGDKVKUWTCGYOA-URGPHPNLSA-N [4-[4-[(z)-c-(4-bromophenyl)-n-ethoxycarbonimidoyl]piperidin-1-yl]-4-methylpiperidin-1-yl]-(2,4-dimethyl-1-oxidopyridin-1-ium-3-yl)methanone Chemical compound C=1C=C(Br)C=CC=1C(=N/OCC)\C(CC1)CCN1C(CC1)(C)CCN1C(=O)C1=C(C)C=C[N+]([O-])=C1C ZGDKVKUWTCGYOA-URGPHPNLSA-N 0.000 claims description 3
239000002955 immunomodulating agent Substances 0.000 claims description 3
229940121354 immunomodulator Drugs 0.000 claims description 3
230000002584 immunomodulator Effects 0.000 claims description 3
239000002777 nucleoside Substances 0.000 claims description 3
238000006467 substitution reaction Methods 0.000 claims description 3
125000004180 3-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(F)=C1[H] 0.000 claims description 2
208000031886 HIV Infections Diseases 0.000 claims description 2
208000037357 HIV infectious disease Diseases 0.000 claims description 2
208000033519 human immunodeficiency virus infectious disease Diseases 0.000 claims description 2
150000003833 nucleoside derivatives Chemical class 0.000 claims description 2
125000004344 phenylpropyl group Chemical group 0.000 claims description 2
GWNOTCOIYUNTQP-FQLXRVMXSA-N 4-[4-[[(3r)-1-butyl-3-[(r)-cyclohexyl(hydroxy)methyl]-2,5-dioxo-1,4,9-triazaspiro[5.5]undecan-9-yl]methyl]phenoxy]benzoic acid Chemical compound N([C@@H](C(=O)N1CCCC)[C@H](O)C2CCCCC2)C(=O)C1(CC1)CCN1CC(C=C1)=CC=C1OC1=CC=C(C(O)=O)C=C1 GWNOTCOIYUNTQP-FQLXRVMXSA-N 0.000 claims 4
ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims 2
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims 2
HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 claims 2
241001529453 unidentified herpesvirus Species 0.000 claims 2
NUUJABLXDPBHDP-UHFFFAOYSA-N 2h-pyran-5-carboxylic acid Chemical compound OC(=O)C1=COCC=C1 NUUJABLXDPBHDP-UHFFFAOYSA-N 0.000 claims 1
240000007594 Oryza sativa Species 0.000 claims 1
235000007164 Oryza sativa Nutrition 0.000 claims 1
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RWTNPBWLLIMQHL-UHFFFAOYSA-N fexofenadine Chemical compound C1=CC(C(C)(C(O)=O)C)=CC=C1C(O)CCCN1CCC(C(O)(C=2C=CC=CC=2)C=2C=CC=CC=2)CC1 RWTNPBWLLIMQHL-UHFFFAOYSA-N 0.000 claims 1
229930182470 glycoside Natural products 0.000 claims 1
150000002338 glycosides Chemical class 0.000 claims 1
VNXBKJFUJUWOCW-UHFFFAOYSA-N methylcyclopropane Chemical compound CC1CC1 VNXBKJFUJUWOCW-UHFFFAOYSA-N 0.000 claims 1
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239000001294 propane Substances 0.000 claims 1
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235000009566 rice Nutrition 0.000 claims 1
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 180
235000002639 sodium chloride Nutrition 0.000 description 92
235000019439 ethyl acetate Nutrition 0.000 description 87
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OKKJLVBELUTLKV-UHFFFAOYSA-N methanol Natural products OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 79
IAZDPXIOMUYVGZ-WFGJKAKNSA-N Dimethyl sulfoxide Chemical compound [2H]C([2H])([2H])S(=O)C([2H])([2H])[2H] IAZDPXIOMUYVGZ-WFGJKAKNSA-N 0.000 description 76
239000002585 base Substances 0.000 description 73
238000000034 method Methods 0.000 description 68
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 56
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WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 48
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HNQIVZYLYMDVSB-UHFFFAOYSA-N methanesulfonimidic acid Chemical compound CS(N)(=O)=O HNQIVZYLYMDVSB-UHFFFAOYSA-N 0.000 description 35
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QWAXKHKRTORLEM-UGJKXSETSA-N saquinavir Chemical compound C([C@@H]([C@H](O)CN1C[C@H]2CCCC[C@H]2C[C@H]1C(=O)NC(C)(C)C)NC(=O)[C@H](CC(N)=O)NC(=O)C=1N=C2C=CC=CC2=CC=1)C1=CC=CC=C1 QWAXKHKRTORLEM-UGJKXSETSA-N 0.000 description 26
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238000005481 NMR spectroscopy Methods 0.000 description 20
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YMARZQAQMVYCKC-OEMFJLHTSA-N amprenavir Chemical compound C([C@@H]([C@H](O)CN(CC(C)C)S(=O)(=O)C=1C=CC(N)=CC=1)NC(=O)O[C@@H]1COCC1)C1=CC=CC=C1 YMARZQAQMVYCKC-OEMFJLHTSA-N 0.000 description 17
AXRYRYVKAWYZBR-GASGPIRDSA-N atazanavir Chemical compound C([C@H](NC(=O)[C@@H](NC(=O)OC)C(C)(C)C)[C@@H](O)CN(CC=1C=CC(=CC=1)C=1N=CC=CC=1)NC(=O)[C@@H](NC(=O)OC)C(C)(C)C)C1=CC=CC=C1 AXRYRYVKAWYZBR-GASGPIRDSA-N 0.000 description 17
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RCINICONZNJXQF-MZXODVADSA-N taxol Chemical compound O([C@@H]1[C@@]2(C[C@@H](C(C)=C(C2(C)C)[C@H](C([C@]2(C)[C@@H](O)C[C@H]3OC[C@]3([C@H]21)OC(C)=O)=O)OC(=O)C)OC(=O)[C@H](O)[C@@H](NC(=O)C=1C=CC=CC=1)C=1C=CC=CC=1)O)C(=O)C1=CC=CC=C1 RCINICONZNJXQF-MZXODVADSA-N 0.000 description 1
OQHZMGOXOOOFEE-SYQUUIDJSA-N tert-butyl n-[(2s,3r)-3-hydroxy-4-[[(2r,3s)-2-hydroxy-3-[(2-methylpropan-2-yl)oxycarbonylamino]-4-[4-(2-morpholin-4-yl-2-oxoethoxy)phenyl]butyl]amino]-1-phenylbutan-2-yl]carbamate Chemical compound C([C@H](NC(=O)OC(C)(C)C)[C@H](O)CNC[C@@H](O)[C@H](CC=1C=CC(OCC(=O)N2CCOCC2)=CC=1)NC(=O)OC(C)(C)C)C1=CC=CC=C1 OQHZMGOXOOOFEE-SYQUUIDJSA-N 0.000 description 1
KKRYDPVDJYCEER-QEGGNFSNSA-N tert-butyl n-[(2s,3r)-3-hydroxy-4-[[(2r,3s)-2-hydroxy-3-[(2-methylpropan-2-yl)oxycarbonylamino]-4-phenylbutyl]amino]-1-phenylbutan-2-yl]carbamate Chemical compound C([C@H](NC(=O)OC(C)(C)C)[C@H](O)CNC[C@@H](O)[C@H](CC=1C=CC=CC=1)NC(=O)OC(C)(C)C)C1=CC=CC=C1 KKRYDPVDJYCEER-QEGGNFSNSA-N 0.000 description 1
150000003512 tertiary amines Chemical class 0.000 description 1
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YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
125000001712 tetrahydronaphthyl group Chemical group C1(CCCC2=CC=CC=C12)* 0.000 description 1
125000003831 tetrazolyl group Chemical group 0.000 description 1
229940126585 therapeutic drug Drugs 0.000 description 1
238000002560 therapeutic procedure Methods 0.000 description 1
125000001113 thiadiazolyl group Chemical group 0.000 description 1
125000000335 thiazolyl group Chemical group 0.000 description 1
125000001544 thienyl group Chemical group 0.000 description 1
ZFEAMMNVDPDEGE-LGRGJMMZSA-N tifuvirtide Chemical compound C([C@H](NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC(N)=O)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](C)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](CC(C)C)NC(=O)[C@H](C)NC(=O)[C@@H](NC(=O)[C@@H](NC(=O)[C@H](CCCCN)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CC=1C2=CC=CC=C2NC=1)NC(=O)[C@H](CCC(O)=O)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@H](CC=1C2=CC=CC=C2NC=1)NC(C)=O)[C@@H](C)CC)[C@@H](C)O)[C@@H](C)CC)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CCCCN)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](C)C(=O)N[C@@H](CO)C(=O)N[C@@H](CC(C)C)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CCC(O)=O)C(=O)N[C@@H](CC=1C2=CC=CC=C2NC=1)C(=O)N[C@@H](CC=1C=CC=CC=1)C(N)=O)C1=CC=C(O)C=C1 ZFEAMMNVDPDEGE-LGRGJMMZSA-N 0.000 description 1
239000004408 titanium dioxide Substances 0.000 description 1
231100000331 toxic Toxicity 0.000 description 1
230000002588 toxic effect Effects 0.000 description 1
238000002054 transplantation Methods 0.000 description 1
238000011269 treatment regimen Methods 0.000 description 1
125000004306 triazinyl group Chemical group 0.000 description 1
125000001425 triazolyl group Chemical group 0.000 description 1
QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical class [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
229940029284 trichlorofluoromethane Drugs 0.000 description 1
ZDRNMODJXFOYMN-UHFFFAOYSA-N tridecyl acetate Chemical compound CCCCCCCCCCCCCOC(C)=O ZDRNMODJXFOYMN-UHFFFAOYSA-N 0.000 description 1
UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 description 1
IEDVJHCEMCRBQM-UHFFFAOYSA-N trimethoprim Chemical compound COC1=C(OC)C(OC)=CC(CC=2C(=NC(N)=NC=2)N)=C1 IEDVJHCEMCRBQM-UHFFFAOYSA-N 0.000 description 1
229960001082 trimethoprim Drugs 0.000 description 1
JBWKIWSBJXDJDT-UHFFFAOYSA-N triphenylmethyl chloride Chemical compound C=1C=CC=CC=1C(C=1C=CC=CC=1)(Cl)C1=CC=CC=C1 JBWKIWSBJXDJDT-UHFFFAOYSA-N 0.000 description 1
238000003828 vacuum filtration Methods 0.000 description 1
229940093257 valacyclovir Drugs 0.000 description 1
229940070710 valerate Drugs 0.000 description 1
NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 1
229960002149 valganciclovir Drugs 0.000 description 1
210000003462 vein Anatomy 0.000 description 1
239000010455 vermiculite Substances 0.000 description 1
229910052902 vermiculite Inorganic materials 0.000 description 1
235000019354 vermiculite Nutrition 0.000 description 1
230000029812 viral genome replication Effects 0.000 description 1
230000008673 vomiting Effects 0.000 description 1
BCEHBSKCWLPMDN-MGPLVRAMSA-N voriconazole Chemical compound C1([C@H](C)[C@](O)(CN2N=CN=C2)C=2C(=CC(F)=CC=2)F)=NC=NC=C1F BCEHBSKCWLPMDN-MGPLVRAMSA-N 0.000 description 1
229960004740 voriconazole Drugs 0.000 description 1
239000001993 wax Substances 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
229940100445 wheat starch Drugs 0.000 description 1
229960000523 zalcitabine Drugs 0.000 description 1
229960002555 zidovudine Drugs 0.000 description 1
HBOMLICNUCNMMY-XLPZGREQSA-N zidovudine Chemical compound O=C1NC(=O)C(C)=CN1[C@@H]1O[C@H](CO)[C@@H](N=[N+]=[N-])C1 HBOMLICNUCNMMY-XLPZGREQSA-N 0.000 description 1
229910052725 zinc Inorganic materials 0.000 description 1
239000011701 zinc Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
- A61P31/18—Antivirals for RNA viruses for HIV
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings

Landscapes

Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Virology (AREA)
Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
Pharmacology & Pharmacy (AREA)
Oncology (AREA)
Molecular Biology (AREA)
Chemical Kinetics & Catalysis (AREA)
General Chemical & Material Sciences (AREA)
Medicinal Chemistry (AREA)
Tropical Medicine & Parasitology (AREA)
AIDS & HIV (AREA)
Communicable Diseases (AREA)
Animal Behavior & Ethology (AREA)
General Health & Medical Sciences (AREA)
Public Health (AREA)
Veterinary Medicine (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Plural Heterocyclic Compounds (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

TW096124262A 2006-07-05 2007-07-04 Therapeutic compounds TWI334867B (en)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date
US80659606P	2006-07-05	2006-07-05
US91098807P	2007-04-10	2007-04-10
US94180807P	2007-06-04	2007-06-04

Publications (2)

Publication Number	Publication Date
TW200811159A TW200811159A (en)	2008-03-01
TWI334867B true TWI334867B (en)	2010-12-21

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ID=38515807

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TW096124262A TWI334867B (en)	2006-07-05	2007-07-04	Therapeutic compounds

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US (1)	US7919488B2 (sr)
EP (1)	EP2046774A1 (sr)
KR (1)	KR20090034958A (sr)
CN (1)	CN101511812A (sr)
AP (1)	AP2009004763A0 (sr)
AR (1)	AR062154A1 (sr)
AU (1)	AU2007270814B2 (sr)
CA (1)	CA2660031A1 (sr)
CO (1)	CO6150178A2 (sr)
CR (1)	CR10573A (sr)
EA (1)	EA200900135A1 (sr)
GT (1)	GT200700053A (sr)
IL (1)	IL196490A0 (sr)
MA (1)	MA30629B1 (sr)
MX (1)	MX2009000482A (sr)
NO (1)	NO20090346L (sr)
NZ (1)	NZ574207A (sr)
PE (1)	PE20080998A1 (sr)
RS (1)	RS20090036A (sr)
TN (1)	TN2009000033A1 (sr)
TW (1)	TWI334867B (sr)
UY (1)	UY30460A1 (sr)
WO (1)	WO2008004096A1 (sr)
ZA (1)	ZA200900478B (sr)

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CN101534824A (zh) *	2006-11-17	2009-09-16	艾博特公司	作为化学活素受体拮抗剂的氨基吡咯烷
EP2132176A1 (en) *	2007-03-13	2009-12-16	Arete Therapeutics, Inc.	4-piperidinylurea compounds as soluble epoxide hydrolase inhibitors
EP2257536A4 (en)	2008-02-14	2011-03-23	Amira Pharmaceuticals Inc	CYCLIC DIARYL ETHERS AS ANTAGONISTS OF PROSTAGLANDIN D2 RECEPTORS
US8426449B2 (en)	2008-04-02	2013-04-23	Panmira Pharmaceuticals, Llc	Aminoalkylphenyl antagonists of prostaglandin D2 receptors
DE102008057343A1 (de)	2008-11-14	2010-05-20	Bayer Schering Pharma Aktiengesellschaft	Heterocyclisch substituierte Aryl-Verbindungen und ihre Verwendung
DE102009041241A1 (de)	2009-09-11	2011-08-04	Bayer Schering Pharma Aktiengesellschaft, 13353	Substituierte Aryl-Verbindungen und ihre Verwendung
DE102008057364A1 (de)	2008-11-14	2010-05-20	Bayer Schering Pharma Aktiengesellschaft	Substituierte Aryl-Verbindungen und ihre Verwendung
DE102009041242A1 (de)	2009-09-11	2011-12-15	Bayer Schering Pharma Aktiengesellschaft	Heterocyclisch substituierte Aryl-Verbindungen und ihre Verwendung
DE102008057344A1 (de)	2008-11-14	2010-05-20	Bayer Schering Pharma Aktiengesellschaft	Aminoalkyl-substituierte Aryl-Verbindungen und ihre Verwendung
WO2010057118A2 (en)	2008-11-17	2010-05-20	Amira Pharmaceuticals, Inc.	Heterocyclic antagonists of prostaglandin d2 receptors
WO2012003405A1 (en)	2010-06-30	2012-01-05	Ironwood Pharmaceuticals, Inc.	Sgc stimulators
NZ609955A (en)	2010-11-09	2015-05-29	Ironwood Pharmaceuticals Inc	Sgc stimulators
CN104066731B (zh)	2011-12-27	2016-06-15	铁木医药有限公司	可用作sgc刺激剂的2-苄基、3-(嘧啶-2-基)取代的吡唑类
CN104540813A (zh) *	2012-06-27	2015-04-22	默沙东公司	磺酰胺衍生物以及使用它们用于改善药物的药物动力学的方法
WO2014000178A1 (en)	2012-06-27	2014-01-03	Merck Sharp & Dohme Corp.	Sulfonamide derivatives and methods of use thereof for improving the pharmacokinetics of a drug
WO2014194519A1 (en) *	2013-06-07	2014-12-11	Merck Sharp & Dohme Corp.	Imidazole derivatives and methods of use thereof for improving pharmacokinetics of drug
WO2015070366A1 (en)	2013-11-12	2015-05-21	Merck Sharp & Dohme Corp.	Aryl linked imidazole and triazole derivatives and methods of use thereof for improving the pharmacokinetics of a drug
WO2015070367A1 (en)	2013-11-12	2015-05-21	Merck Sharp & Dohme Corp.	Piperidine or piperazine linked imidazole and triazole derivatives and methods of use thereof for improving the pharmacokinetics of a drug
WO2020163689A1 (en) *	2019-02-08	2020-08-13	University Of Pittsburgh - Of The Commonwealth System Of Higher Education	20-hete formation inhibitors

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GB0024795D0 (en) *	2000-10-10	2000-11-22	Hoffmann La Roche	Pyrazole derivatives for the treatment of viral diseases
KR100785109B1 (ko) *	2001-04-05	2007-12-12	토렌트 파마슈티칼스 리미티드	노화 관련 및 당뇨병 혈관성 합병증에 사용되는 헤테로사이클릭 화합물
US7008953B2 (en) *	2003-07-30	2006-03-07	Agouron Pharmaceuticals, Inc.	3, 5 Disubstituted indazole compounds, pharmaceutical compositions, and methods for mediating or inhibiting cell proliferation
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ES2340200T3 (es) *	2005-09-23	2010-05-31	Pfizer Products Inc.	Benzamidas sustituidas con piridinaminosulfonil como inhibidores de citromo p450 3a4 (cyp3a4).

2007
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- 2007-06-25 EP EP07734950A patent/EP2046774A1/en not_active Withdrawn
- 2007-06-25 AU AU2007270814A patent/AU2007270814B2/en not_active Ceased
- 2007-06-25 CN CNA200780032889XA patent/CN101511812A/zh active Pending
- 2007-06-25 CA CA002660031A patent/CA2660031A1/en not_active Abandoned
- 2007-06-25 WO PCT/IB2007/001878 patent/WO2008004096A1/en not_active Ceased
- 2007-06-25 MX MX2009000482A patent/MX2009000482A/es not_active Application Discontinuation
- 2007-06-25 AP AP2009004763A patent/AP2009004763A0/xx unknown
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- 2007-06-25 NZ NZ574207A patent/NZ574207A/en not_active IP Right Cessation
- 2007-06-25 KR KR1020097002315A patent/KR20090034958A/ko not_active Ceased
- 2007-06-28 US US11/770,698 patent/US7919488B2/en not_active Expired - Fee Related
- 2007-07-03 AR ARP070102977A patent/AR062154A1/es not_active Application Discontinuation
- 2007-07-04 UY UY30460A patent/UY30460A1/es unknown
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Also Published As

Publication number	Publication date
EA200900135A1 (ru)	2009-06-30
MA30629B1 (fr)	2009-08-03
AU2007270814B2 (en)	2011-07-14
KR20090034958A (ko)	2009-04-08
AP2009004763A0 (en)	2009-02-28
TW200811159A (en)	2008-03-01
IL196490A0 (en)	2011-07-31
UY30460A1 (es)	2008-02-29
PE20080998A1 (es)	2008-08-15
CO6150178A2 (es)	2010-04-20
CR10573A (es)	2009-02-12
NZ574207A (en)	2010-10-29
WO2008004096A1 (en)	2008-01-10
EP2046774A1 (en)	2009-04-15
US20080021011A1 (en)	2008-01-24
MX2009000482A (es)	2009-01-27
AR062154A1 (es)	2008-10-22
US7919488B2 (en)	2011-04-05
GT200700053A (es)	2009-08-03
RS20090036A (sr)	2010-06-30
CA2660031A1 (en)	2008-01-10
CN101511812A (zh)	2009-08-19
ZA200900478B (en)	2010-04-28
TN2009000033A1 (fr)	2010-08-19
AU2007270814A1 (en)	2008-01-10
NO20090346L (no)	2009-02-19

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2013-09-21	MM4A	Annulment or lapse of patent due to non-payment of fees

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